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A patient with Rhupus was diagnosed with Rowell syndrome and treated with various medications.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Researchers developed a new way to measure gene activity in single hair follicles and found that a specific gene's activity changes with different amounts and times of treatment.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Scientists made glow-in-the-dark dots from human hair that can detect iron, prevent counterfeiting, and reveal fingerprints.

Laser ablation ICP-MS is effective for tracking trace elements in polar bear hair over time.

The woman had a genetic condition causing high cortisol and androgen levels, treatable with dexamethasone.

The method greatly improves low-light sports images' quality and reduces artifacts.

Using human recombinant hyaluronidase in donor strip harvesting may improve the procedure.

Innovative methods are reducing animal testing and improving biomedical research.

The GH-IGF-I axis is likely involved in the hormonal imbalances seen in non-obese women with functional hyperandrogenism.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Dermoscopy can help assess the severity of chronic radiation-induced skin damage in head and neck cancer patients.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

A new method accurately measures long-term hormone levels in hair.

Hair cortisol measurement is a promising, non-invasive tool for monitoring cortisol exposure over time.

Distal hair cortisol is not a reliable measure of early pregnancy cortisol levels.

OsPHR2 gene in rice enhances root growth and phosphorus accumulation.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

Scientists created iodinated arylhydantoins and arylthiohydantoins that could potentially be used for imaging prostate cancer. Some versions with specific side-chains showed high potential for this use.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Certain surgical methods are better than routine incision for hidradenitis suppurativa, topical clindamycin and acitretin are effective treatments, men with HS have a risk of skin cancer, HS patients are more likely to die from heart problems, and specific genetic markers are linked to treatment response.

More research is needed to understand and manage rheumatoid arthritis better.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Airway issues can occur in Conradi–Hünermann–Happle syndrome and can be managed with minimally invasive procedures.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Mutations in the hHb6 gene cause the hair disorder monilethrix.